Effect of an oral iron chelator or iron-deficient diets on uroporphyria in a murine model of porphyria cutanea tarda
Author:
Publisher
Wiley
Subject
Hepatology
Reference32 articles.
1. Biosynthesis of heme in mammals;Ajioka;Biochim Biophys Acta,2006
2. Porphyria cutanea tarda: multiplicity of risk factors including HFE mutations, hepatitis C, and inherited uroporphyrinogen decarboxylase deficiency;Egger;Dig Dis Sci,2002
3. Co-inheritance of mutations in the uroporphyrinogen decarboxylase and hemochromatosis genes accelerates the onset of porphyria cutanea tarda;Brady;J Invest Dermatol,2000
4. C282Y and H63D mutation of the hemochromatosis gene in German porphyria cutanea tarda patients;Tannapfel;Virchows Arch,2001
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1. Relapse of porphyria cutanea tarda after treatment with phlebotomy or 4-aminoquinoline antimalarials: a meta-analysis;British Journal of Dermatology;2018-07-26
2. Iron overload in hereditary tyrosinemia type 1 induces liver injury through the Sp1/Tfr2/hepcidin axis;Journal of Hepatology;2016-07
3. Antioxidant targeting by deferiprone in diseases related to oxidative damage;Frontiers in Bioscience;2014
4. Non-Hfe Iron Overload: Is Phlebotomy the Answer?;Current Hepatitis Reports;2012-12-11
5. Low-Dose Hydroxychloroquine Is as Effective as Phlebotomy in Treatment of Patients With Porphyria Cutanea Tarda;Clinical Gastroenterology and Hepatology;2012-12
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